Canonical Allele Identifier: CA449776478

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691571C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723794C>T , CM000668.2:g.30723794C>T	GRCh38
NC_000006.11:g.30691571C>T , CM000668.1:g.30691571C>T	GRCh37
NC_000006.10:g.30799550C>T	NCBI36
NG_034142.1:g.8594C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.732C>T MANE Select	ENSP00000339001.7:p.Gly244=
ENST00000680530.1:n.1594C>T
ENST00000681421.1:n.1798C>T
ENST00000681435.1:c.516C>T	ENSP00000506665.1:p.Gly172=
ENST00000327892.12:c.732C>T	ENSP00000339001.7:p.Gly244=
ENST00000330914.7:c.516C>T	ENSP00000365578.2:p.Gly172=
ENST00000396384.1:c.516C>T	ENSP00000379668.1:p.Gly172=
ENST00000396389.5:c.678C>T	ENSP00000379672.1:p.Gly226=
NM_001293212.1:c.792C>T	NP_001280141.1:p.Gly264=
NM_001293213.1:c.370-244C>T	NP_001280142.1:n.370-244C>T
NM_001293214.1:c.600C>T	NP_001280143.1:p.Gly200=
NM_001293215.1:c.516C>T	NP_001280144.1:p.Gly172=
NM_001293216.1:c.516C>T	NP_001280145.1:p.Gly172=
NM_178014.3:c.732C>T	NP_821133.1:p.Gly244=
NR_120608.1:n.584-145C>T
NM_178014.4:c.732C>T MANE Select	NP_821133.1:p.Gly244=
NM_001293212.2:c.792C>T	NP_001280141.1:p.Gly264=
NM_001293213.2:c.370-244C>T	NP_001280142.1:n.370-244C>T
NM_001293214.2:c.600C>T	NP_001280143.1:p.Gly200=
NM_001293215.2:c.516C>T	NP_001280144.1:p.Gly172=
NM_001293216.2:c.516C>T	NP_001280145.1:p.Gly172=
NR_120608.2:n.433-145C>T